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» Authors » Phan Tuong Quynh Le

Phan Tuong Quynh Le

Explore the profile of Phan Tuong Quynh Le including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 7
Citations 20
Followers 0
Related Specialties
General Medicine
Oncology
Endocrinology
Top 10 Co-Authors
Thi Minh Thi Ha
Van Huy Tran
Thanh Nha Uyen Le
Viet Nhan Nguyen
Trung Nam Phan
Trong Hieu Nguyen
Huu Nhat Binh Doan
Hoai-Nghia Nguyen
Dac Ho Vo
Le Son Tran
Published In
J Glob Antimicrob Resist
Nagoya J Med Sci
Case Rep Endocrinol
J Infect Dev Ctries
Future Oncol
Affiliations
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Recent Articles
1.
Evaluation of a multimodal ctDNA-based assay for detection of aggressive cancers lacking standard screening tests
Thien Nguyen C, Nguyen T, Vo D, Van T, Nguyen G, Tran T, et al.
Future Oncol . 2024 Oct; 21(1):105-115. PMID: 39431470
Cancers lacking standard screening (LSS) options account for approximately 70% of cancer-related deaths due to late-stage diagnosis. Circulating tumor DNA (ctDNA) is a promising biomarker for multi-cancer early detection. We...
2.
Current status of Helicobacter pylori resistance to clarithromycin and levofloxacin in Vietnam: Results from molecular analysis of gastric biopsy specimens
Tran V, Nguyen T, Quynh Le P, Nguyen T, Nguyen T, Thi Ha T
J Glob Antimicrob Resist . 2023 Dec; 36:76-82. PMID: 38160708
Objectives: The management of Helicobacter pylori in Vietnam is becoming progressively more difficult due to increasing antibiotic resistance, particularly to clarithromycin (CLR) and levofloxaxin (LVX). In Vietnam, the selection of...
3.
An extremely rare missense mutation of the androgen receptor gene in a Vietnamese family with complete androgen insensitivity syndrome
Thi Ha T, Quynh Le P, Le T, Hoang T
Nagoya J Med Sci . 2023 Jun; 85(2):362-368. PMID: 37346838
We report a Vietnamese family with complete androgen insensitivity syndrome that included several phenotypic females who have a 46,XY karyotype with an extremely rare mutation of the androgen receptor gene....
4.
An Extremely Rare Gene c.485A>C Mutation in a Compound Heterozygous Newborn with Disorders of Sex Development First Identified in Vietnam
Quynh Le P, Le T, Nguyen T, Nguyen M, Thi Ha T
Case Rep Endocrinol . 2022 Apr; 2022:6025916. PMID: 35386187
(steroid 5-alpha-reductase 2) mutation, which impairs 5-reductase-2 enzyme activity, is among the causes of 46,XY disorders of sex development (DSD). Here, we report a rare pathogenic mutation NM_000348.4:c.485A>C (NP_000339.2:p.His162Pro) of...
5.
An experience in prenatal diagnosis via QF-PCR of a female child with a 9.9 Mb pure deletion at 18p11.32-11.22
Le T, Nguyen V, Doan T, Doan H, Quynh Le P, Le T, et al.
Nagoya J Med Sci . 2020 Dec; 82(4):783-790. PMID: 33311808
Quantitative Fluorescent - Polymerase Chain Reaction (QF-PCR) is a rapid prenatal diagnosis test for 21, 18, 13 and sex chromosomal aneuploidy detection. However, it could not detect partial trisomy or...
6.
Helicobacter pylori 23S rRNA gene mutations associated with clarithromycin resistance in chronic gastritis in Vietnam
Tran V, Thi Ha T, Quynh Le P, Nguyen V, Phan T, Paglietti B
J Infect Dev Ctries . 2020 Jan; 12(7):526-532. PMID: 31954001
Introduction: Data about the prevalence of the A2142C, A2142G, and A2143G mutations in 23S rRNA gene is still limited. The aim of this study was to determine the prevalence of...
7.
Characterisation of point mutations in domain V of the 23S rRNA gene of clinical Helicobacter pylori strains and clarithromycin-resistant phenotype in central Vietnam
Tran V, Thi Ha T, Quynh Le P, Phan T, Tran T
J Glob Antimicrob Resist . 2018 Sep; 16:87-91. PMID: 30266639
Objectives: The prevalence of clarithromycin (CLR)-resistant Helicobacter pylori is increasing worldwide, including in Vietnam. The aims of this study were to determine point mutations in the 23S rRNA domain V...